International Classification of Diseases, Version 10 - Clinical Modification - Hereditary retinal dystrophy - Classes

Last uploaded: January 29, 2019

Preferred Name	Hereditary retinal dystrophy
ID	http://purl.bioontology.org/ontology/ICD10CM/H35.5
cui	C0154860
EXCLUDES1	dystrophies primarily involving Bruch's membrane (H31.1-)
Inverse of SIB	http://purl.bioontology.org/ontology/ICD10CM/H35.3 http://purl.bioontology.org/ontology/ICD10CM/H35.0 http://purl.bioontology.org/ontology/ICD10CM/H35.8 http://purl.bioontology.org/ontology/ICD10CM/H35.2 http://purl.bioontology.org/ontology/ICD10CM/H35.7 http://purl.bioontology.org/ontology/ICD10CM/H35.1 http://purl.bioontology.org/ontology/ICD10CM/H35.6 http://purl.bioontology.org/ontology/ICD10CM/H35.4 http://purl.bioontology.org/ontology/ICD10CM/H35.9
notation	H35.5
Order number	08730
prefLabel	Hereditary retinal dystrophy
tui	T047
subClassOf	http://purl.bioontology.org/ontology/ICD10CM/H35

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bmicc.cn/ontology/ICD10CN/H35.5	International Classification of Diseases, 10th Edition, China	CUI
http://purl.obolibrary.org/obo/DOID_8500	Human Disease Ontology 123	LOOM
http://purl.bioontology.org/ontology/ICD10/H35.5	International Classification of Diseases, Version 10	CUI
http://purl.bioontology.org/ontology/ICD10/H35.5	International Classification of Diseases, Version 10	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C35194	National Cancer Institute Thesaurus	LOOM